This next month will mark 24 years since I joined the MAGIC Foundation family, first as the Russell-Silver syndrome (RSS) division consultant and later starting the RSS/SGA Research & Education unit within MAGIC. We felt strongly then, and now, that patients and families should have access to the most up-to-date information on diagnosis and treatment regardless of where they live or income level. My daughter (who has RSS) is now an adult; graduated college, married and working in public health overseas. She has benefitted from our association with MAGIC and both of us have decades-long friendships through MAGIC. Our lives have been changed for the better thanks to the founders of MAGIC and the dedicated staff, volunteers and associated physicians who work so hard to help families.